Combination of Exchange Transfusion Treatment and Hydroxyurea Cause Beneficial Changes to Laboratory Parameters and Clinical Outcome in Patients with Sickle Cell Disease/β Thalassemia Compared with Hydroxyurea or Exchange Transfusion Alone

Author:

Delicou Sophia

Publisher

MedCrave Group, LLC

Subject

General Medicine

Reference36 articles.

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2. Hydroxyurea for the treatment of sickle cell anemia;Platt;N Engl J Med,2008

3. Weatherall D, Akinyanju O, Fucharoen S, et al. Inherited disorders of hemoglobin. In: Jamison DT, et al. editors. Disease Control Priorities in Developing Countries. 2nd ed. Washington, USA: World bankl; 2006.

4. Sickle-cell disease;Rees;Lancet,2010

5. Yale SH, Nagib N, Guthrie T. Approach to the vaso-occlusive crisis in adults with sickle cell disease. Am Fam Physician. 2000;61(5):1349–1356.

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